Smoothing method for cleaved films made using a release layer

Information

  • Patent Grant
  • 6391219
  • Patent Number
    6,391,219
  • Date Filed
    Friday, July 30, 1999
    24 years ago
  • Date Issued
    Tuesday, May 21, 2002
    22 years ago
Abstract
A method for treating a film of material, which can be defined on a substrate, e.g., silicon. The method includes providing a substrate comprising a cleaved surface, which had a porous silicon layer thereon. The substrate may have a distribution of hydrogen bearing particles defined from the cleaved surface to a region underlying said cleaved surface. The method also includes increasing a temperature of the cleaved surface to greater than about 1,000 Degrees Celsius while maintaining the cleaved surface in a etchant bearing environment to reduce a surface roughness value by about fifty percent and greater. Preferably, the value can be reduced by about eighty or ninety percent and greater, depending upon the embodiment.
Description




BACKGROUND OF THE INVENTION




The present invention relates to the manufacture of objects. More particularly, the present invention provides a technique for improving surface texture or surface characteristics of a film of material, e.g., silicon, silicon germanium, or others. The present invention can be applied to treating or smoothing a cleaved film from a layer transfer process for the manufacture of integrated circuits, for example. But it will be recognized that the invention has a wider range of applicability; it can also be applied to smoothing a film for other substrates such as multi-layered integrated circuit devices, three-dimensional packaging of integrated semiconductor devices, photonic devices, piezoelectronic devices, microelectromechanical systems (“MEMS”), sensors, actuators, solar cells, flat panel displays (e.g., LCD, AMLCD), doping semiconductor devices, biological and biomedical devices, and the like.




Integrated circuits are fabricated on chips of semiconductor material. These integrated circuits often contain thousands, or even millions, of transistors and other devices. In particular, it is desirable to put as many transistors as possible within a given area of semiconductor because more transistors typically provide greater functionality, and a smaller chip means more chips per wafer and lower costs. Some integrated circuits are fabricated on a slice or wafer, of single-crystal (monocrystalline) silicon, commonly termed a “bulk” silicon wafer. Devices on such “bulk” silicon wafer typically are isolated from each other. A variety of techniques have been proposed or used to isolate these devices from each other on the bulk silicon wafer, such as a local oxidation of silicon (“LOCOS”) process, trench isolation, and others. These techniques, however, are not free from limitations. For example, conventional isolation techniques consume a considerable amount of valuable wafer surface area on the chip, and often generate a non-planar surface as an artifact of the isolation process. Either or both of these considerations generally limit the degree of integration achievable in a given chip. Additionally, trench isolation often requires a process of reactive ion etching, which is extremely time consuming and can be difficult to achieve accurately.




An approach to achieving very-large scale integration (“VLSI”) or ultra-large scale integration (“ULSI”) is by using a semiconductor-on-insulator (“SOI”) wafer. An SOI wafer typically has a layer of silicon on top of a layer of an insulator material. A variety of techniques have been proposed or used for fabricating the SOI wafer. These techniques include, among others, growing a thin layer of silicon on a sapphire substrate, bonding a layer of silicon to an insulating substrate, and forming an insulating layer beneath a silicon layer in a bulk silicon wafer. In an SOI integrated circuit, essentially complete device isolation is often achieved using conventional device processing methods by surrounding each device, including the bottom of the device, with an insulator. An advantage SOI wafers have over bulk silicon wafers is that the area required for isolation between devices on an SOI wafer is less than the area typically required for isolation on a bulk silicon wafer.




SOI offers other advantages over bulk silicon technologies as well. For example, SOI offers a simpler fabrication sequence compared to a bulk silicon wafer. Devices fabricated on an SOI wafer may also have better radiation resistance, less photo-induced current, and less cross-talk than devices fabricated on bulk silicon wafers. Many problems, however, that have already been solved regarding fabricating devices on bulk silicon wafers remain to be solved for fabricating devices on SOI wafers.




For example, SOI wafers generally must also be polished to remove any surface irregularities from the film of silicon overlying the insulating layer. Polishing generally includes, among others, chemical mechanical polishing, commonly termed CMP. CMP is generally time consuming and expensive, and can be difficult to perform cost efficiently to remove surface non-uniformities. That is, a CMP machine is expensive and requires large quantities of slurry mixture, which is also expensive. The slurry mixture can also be highly acidic or caustic. Accordingly, the slurry mixture can influence functionality and reliability of devices that are fabricated on the SOI wafer.




From the above, it is seen that an improved technique for manufacturing a substrate such as an SOI wafer is highly desirable.




SUMMARY OF THE INVENTION




According to the present invention, a technique for treating a film of material is provided. More particularly, the present invention provides a method for treating a cleaved surface and/or an implanted surface using a combination of thermal treatment and chemical reaction, which can form a substantially smooth film layer from the cleaved surface.




In a specific embodiment, the present invention provides a method for forming a semiconductor substrate. The method includes forming a first porous silicon layer on at least one surface of a silicon substrate; and forming a second layer having a larger porosity than the first porous silicon layer at a constant depth from a surface of the porous silicon in the first porous silicon layer. The second layer forming step comprising implanting ions into the first porous silicon layer with a given projection range. The method also includes bonding the non-porous layer and a support substrate together. Next, the method includes a step of separating the silicon substrate into two portions at the second layer to remove the porous silicon layer exposed on a surface of the support substrate and exposing the non-porous layer. The method includes smoothing the non-porous layer by subjecting surface(s) of the non-porous layer using an etchant species (e.g., HCl) and thermal treatment. The present substrate can be maintained at 1 atmosphere in some embodiments.




Numerous benefits are achieved by way of the present invention over pre-existing techniques. For example, the present invention provides an efficient technique for forming a substantially uniform surface on an SOI wafer. Additionally, the substantially uniform surface is made by way of common hydrogen treatment and etching techniques, which can be found in conventional epitaxial tools. Furthermore, the present invention provides a novel uniform layer, which can be ready for the manufacture of integrated circuits. The present invention also relies upon standard fabrication gases such as HCl and hydrogen gas. In preferred embodiments, the present invention can improve bond interface integrity, improve crystal structure, and reduce defects in the substrate simultaneously during the process. Depending upon the embodiment, one or more of these benefits is present. These and other advantages or benefits are described throughout the present specification and are described more particularly below.




These and other embodiments of the present invention, as well as its advantages and features are described in more detail in conjunction with the text below and attached Figs.











BRIEF DESCRIPTION OF THE DRAWINGS





FIGS. 1A

to


1


D are schematic diagrams for explaining a semiconductor substrate producing process according to an embodiment of the present invention;





FIGS. 2A

to


2


G are schematic diagrams for explaining a semiconductor substrate producing process according to an embodiment of the present invention;





FIGS. 3A

to


3


F are schematic diagrams for explaining a semiconductor substrate producing process according to an embodiment of the present invention;





FIGS. 4A

to


4


E are schematic diagrams for explaining a semiconductor substrate producing process according to an embodiment of the present invention;





FIGS. 5A

to


5


G are schematic diagrams for explaining a semiconductor substrate producing process according to an embodiment of the present invention;





FIGS. 6A and 6G

are schematic diagrams for explaining a semiconductor substrate producing process according to an embodiment of the present invention; and





FIGS. 7A and 7B

are simplified side-view diagrams of anodization systems according to an embodiment of the present invention











DESCRIPTION OF THE SPECIFIC EMBODIMENT




According to the present invention, a technique for treating a film of material is provided. More particularly, the present invention provides a method for treating a cleaved surface and/or an implanted surface using a combination of thermal treatment and chemical reaction, which can form a substantially smooth film layer from the cleaved surface. The invention will be better understood by reference to the Figs. and the descriptions below.




As shown in

FIG. 1A

, a silicon single-crystal substrate


21


is first prepared and then rendered porous at its surface layer. Numeral


22


denotes the resulting porous layer. As shown in

FIG. 1B

, at least one kind of noble gas, hydrogen and nitrogen is ion-implanted into the porous layer


22


. Then, a porous layer (ion-implanted layer)


23


having large porosity is formed in the porous layer


22


. The charge condition of the implanted ions is not particularly limited. The acceleration energy is set such that the projection range corresponds to a depth at which the ion implantation is desired. Depending on the implantation amount, the size and the density of the micro-cavities to be formed are changed, but approximately no less than 1×10


14


/cm


2


and more preferably 1×10


15


/cm


2


. When setting the projection range to be deeper, the channeling ion implantation may be employed. After the implantation, the heat treatment is performed or at least one of compressive, tensile and shear stresses is applied to the wafer in a direction perpendicular to the surface as necessary, so as to divide the semiconductor substrate into two at the ion-implanted layer as a border. In the case of the heat treatment atmosphere being an oxidizing atmosphere, the pore walls are oxidized so that attention should be given to preventing the silicon region from being all changed into silicon oxide due to over oxidation.




In

FIG. 1C

, the extremely thin porous substrate obtained by the present invention is shown. Since the division of the substrate starts spontaneously upon the heat treatment or the like as a trigger due to the internal stress introduced upon the implantation, the extremely thin porous structure can be formed uniformly all over the substrate. The pores of the porous structure are formed from one main surface of the substrate toward the other main surface. Accordingly, when the gas is implanted under pressure from the one main surface, it is ejected out from the other main surface. In this case, since the pore size of the porous structure is in the range from several nanometers to several tens of nanometers, a particle greater than this can not pass therethrough. On the other hand, although pressure loss is caused depending on the pore size, the pore density and a thickness of the extremely thin porous substrate, the strength of the substrate and the pressure loss can be both within the practical range if the thickness of the porous layer is approximately no more than


20


microns.




As shown in

FIG. 1D

, porous layer


22


, which has an overlying layer


23


, is subjected to further processing. Here, layer


23


is removed by etching techniques. Once layer


23


is removed, a surface treatment process


24


is provided. The surface treatment process removes surface roughness from the surface


25


of the porous layer. The film of silicon material is often rough


25


and needs finishing. The rough surface for silicon wafers is often about two to eight nanometers RMS or greater. This roughness often should be removed before further processing. In a specific embodiment, the detached surface has a concentration of hydrogen bearing particles therein and thereon from the previous implanting step.




To smooth or treat the surface, the substrate is subjected to thermal treatment in a hydrogen bearing environment. Additionally, the substrate is also subjected to an etchant including a halogen bearing compound such as HCl, HBr, HI, HF, and others. The etchant can also be a fluorine bearing compound such as SF


6


or C


x


F


x


. In preferred embodiments, the present substrate undergoes treatment using a combination of etchant and thermal treatment in a hydrogen bearing environment. In a specific embodiment, the etchant is HCl gas or the like. The thermal treatment uses a hydrogen etchant gas. In some embodiments, the etchant gas is a halogenated gas, e.g., HCl, HF, HI, HBr, SF


6


, CF


4


, NF


3


, and CCl


2


F


2


. The etchant gas can also be mixed with another halogen gas, e.g., chlorine, fluorine. The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




In one embodiment, it is believed that the hydrogen particles in the detached surface improves the surface smoothing process. Here, the hydrogen particles have been maintained at a temperature where they have not diffused out of the substrate. In a specific embodiment, the concentration of hydrogen particles ranges from about 10


21


to about 5×10


22


atoms/cm


3


. Alternatively, the concentration of hydrogen particles is at least about 6×10


21


atoms/cm


3


. Depending upon the embodiment, the particular concentration of the hydrogen particles can be adjusted.




Still further in other embodiments, the present substrate undergoes a process of hydrogen treatment or implantation before thermal treatment purposes. Here, the substrate, including the detached film, is subjected to hydrogen bearing particles by way of implantation, diffusion, or any combination thereof. In some embodiments, where hydrogen has diffused out from the initial implant, a subsequent hydrogen treatment process can occur to increase a concentration of hydrogen in the detached film. The present hydrogen treatment process can occur for substrates made by way of other processes such as those noted below.




Moreover, the present technique for finishing the cleaved surface can use a combination of etchant, deposition, and thermal treatment to smooth the cleaved film. Here, the cleaved film is subjected to hydrogen bearing compounds such as HCl, HBr, HI, HF, and others. Additionally, the cleaved film is subjected to for example, deposition, during a time that the film is subjected to the hydrogen bearing compounds, which etch portions of the cleaved film. Using a silicon cleaved film for example, the deposition may occur by way of a silicon bearing compound such as silanes, e.g., Si


x


Cl


y


H


z


, SiH


4


, SiCl


x


, and other silicon compounds. Accordingly, the present method subjects the cleaved film to a combination of etching and deposition using a hydrogen bearing compound and a silicon bearing compound. Additionally, the cleaved surface undergoes thermal treatment while being subjected to the combination of etchant and deposition gases. The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




As shown in

FIG. 2A

, a silicon single-crystal substrate


41


is first prepared and then rendered porous at its surface layer. Numeral


42


denotes the resulting porous layer. Subsequently, as shown in

FIG. 2B

, at least one non-porous thin film


43


is formed on the porous layer. The film to be formed is arbitrarily selected from among a single-crystal silicon film, a polycrystalline silicon film, an amorphous silicon film, a metal film, a compound semiconductor film, a superconductive film, and the like. Alternatively, an element structure such as a MOSFET may be formed.




As shown in

FIG. 2C

, at least one kind of noble gas, hydrogen and nitrogen is ion-implanted into the porous layer


42


so as to form an implanted layer


44


. When observing the implanted layer by a transmission electron microscope, formation of numberless micro-cavities can be seen. The charge condition of the implanted ions is not particularly limited. The acceleration energy is set such that the projection range corresponds to a depth at which the ion implantation is desired. Depending on the implantation amount, the size and the density of the micro-cavities to be formed are changed, but approximately no less than 1×10


14


/cm


2


and more preferably 1×10


15


/cm


2


. When setting the projection range to be deeper, the channeling ion implantation may be employed. After the implantation, the heat treatment is performed as necessary. In case of the heat treatment atmosphere being the oxidizing atmosphere, the pore walls are oxidized so that attention should be given to preventing the silicon region from being all changed into silicon oxide due to over oxidation.




As shown in

FIG. 2D

, after abutting a support substrate


45


and the surface of the first substrate with each other at room temperature, they are bonded to each other through anodic bonding, pressurization, heat treatment or a combination thereof. As a result, both substrates are firmly coupled with each other.




When single-crystal silicon is deposited, it is preferable to perform the bonding after oxidized silicon is formed on the surface of single-crystal silicon through thermal oxidation or the like. On the other hand, the support substrate can be selected from among a silicon substrate, a silicon substrate with a silicon oxide film formed thereon, a light transmittable substrate such as quartz, a sapphire substrate and the like, but not limited thereto as long as the surface serving for the bonding is fully flat. The bonding may be performed in three plies with an insulating thin plate interposed therebetween.




Subsequently, the substrates are divided at the ion-implanted layer


44


in the porous silicon layer


42


(FIG.


2


E). The structure of the second substrate side includes the porous silicon layer


42


, the non-porous thin film (for example, the single-crystal silicon layer)


43


and the second substrate


45


.




Further, the porous silicon layer


42


is selectively removed. In case of the non-porous thin film being single-crystal silicon, only the porous silicon layer


42


is subjected to the electroless wet chemical etching using at least one of the normal silicon etching liquid, hydrofluoric acid being the porous silicon selective etching liquid, a mixed liquid obtained by adding at least one of alcohol and aqueous hydrogen peroxide water to hydrofluoric acid, buffered hydrofluoric acid, and a mixed liquid obtained by adding at least one of alcohol and aqueous hydrogen peroxide to buffered hydrofluoric acid, so as to render the film formed in advance on the porous layer of the first substrate remain on the second substrate. As described above in detail, only the porous silicon layer can be selectively etched using the normal silicon etching liquid due to the extensive surface area of porous silicon. Alternatively, the porous silicon layer


42


may be removed through selective polishing using the single-crystal silicon layer


43


as a polishing stopper.




In the case where the compound semiconductor layer is formed on the porous layer, only the porous silicon layer


42


is subjected to chemical etching using the etching liquid which has the greater etching speed for silicon relative to the compound semiconductor, so that the thickness-reduced single-crystal compound semiconductor layer


43


remains on the insulating substrate


45


. Alternatively, the porous silicon layer


42


is removed through selective polishing using the single-crystal compound semiconductor layer


43


as a polishing stopper.




In

FIG. 2F

, the semiconductor substrate of the present invention is shown. On the insulating substrate


45


, the non-porous thin film, such as the single-crystal silicon thin film


43


, is formed in a large area all over the wafer, flatly and uniformly reduced in thickness. The semiconductor substrate thus obtained can be suitably used in production of an insulated electronic element.




The silicon single-crystal substrate


41


can be reused as an silicon single-crystal substrate


41


after removing remaining any porous silicon and after performing surface-flattening if the surface flatness makes the substrate unusable. Alternatively, a non-porous thin film may be again formed without removing porous silicon so as to provide the substrate as shown in

FIG. 2B

, which is then subjected to the processes shown in

FIGS. 2C

to


2


F. In embodiments where flattening is desirable, a novel surface processing step is provided, as shown in FIG.


2


G. Alternatively, smoothing or flattening of the single crystal silicon thin film is also provided, as shown in FIG.


2


G.





FIG. 2G

illustrates a surface


47


smoothing step for either surface


46


(


a


) or


46


(


b


) according to an embodiment of the present invention. As show, surface


47


is often rough and needs finishing. The present surface treatment process removes surface roughness from the surface


47


of the porous layer. The film of silicon material is often rough


47


and needs finishing. The rough surface for silicon wafers is often about two to eight nanometers RMS or greater. This roughness often should be removed before further processing. In a specific embodiment, the detached surface has a concentration of hydrogen bearing particles therein and thereon from the previous implanting step.




To smooth or treat the surface, the substrate is subjected to thermal treatment in a hydrogen bearing environment. Additionally, the substrate is also subjected to an etchant including a halogen bearing compound such as HCl, HBr, HI, HF, and others. The etchant can also be a fluorine bearing compound such as SF


6


, C


x


F


x


. In preferred embodiments, the present substrate undergoes treatment using a combination of etchant and thermal treatment in a hydrogen bearing environment. In a specific embodiment, the etchant is HCl gas or the like. The thermal treatment uses a hydrogen etchant gas. In some embodiments, the etchant gas is a halogenated gas, e.g., HCl, HF, HI, HBr, SF


6


, CF


4


, NF


3


, and CCl


2


F


2


. The etchant gas can also be mixed with another halogen gas, e.g., chlorine, fluorine. The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be from an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




In one embodiment, it is believed that the hydrogen particles in the detached surface improves the surface smoothing process. Here, the hydrogen particles have been maintained at a temperature where they have not diffused out of the substrate. In a specific embodiment, the concentration of hydrogen particles ranges from about 10


21


to about 5×10


22


atoms/cm


3


. Alternatively, the concentration of hydrogen particles is at least about 6×10


21


atoms/cm


3


. Depending upon the embodiment, the particular concentration of the hydrogen particles can be adjusted.




Still further in other embodiments, the present substrate undergoes a process of hydrogen treatment or implantation before thermal treatment purposes. Here, the substrate, including the detached film, is subjected to hydrogen bearing particles by way of implantation, diffusion, or any combination thereof. In some embodiments, where hydrogen has diffused out from the initial implant, a subsequent hydrogen treatment process can occur to increase a concentration of hydrogen in the detached film. The present hydrogen treatment process can occur for substrates made by way of other processes such as those noted below.




Moreover, the present technique for finishing the cleaved surface can use a combination of etchant, deposition, and thermal treatment to smooth the cleaved film. Here, the cleaved film is subjected to hydrogen bearing compounds such as HCl, HBr, HI, HF, and others. Additionally, the cleaved film is subjected to for example, deposition, during a time that the film is subjected to the hydrogen bearing compounds, which etch portions of the cleaved film. Using a silicon cleaved film for example, the deposition may occur by way of a silicon bearing compound such as silanes, e.g., Si


x


Cl


y


H


z


, SiH


4


, SiCl


x


, and other silicon compounds. Accordingly, the present method subjects the cleaved film to a combination of etching and deposition using a hydrogen bearing compound and a silicon bearing compound. Additionally, the cleaved surface undergoes thermal treatment while being subjected to the combination of etchant and deposition gases The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




As shown in

FIG. 3A

, a silicon single-crystal substrate


51


is first prepared and then rendered porous at both surface layers thereof. Numerals


52


and


53


denote the obtained porous layers. Subsequently, as shown in

FIG. 3B

, at least one non-porous thin film


54


,


55


is formed on each of the porous layers. The film to be formed is arbitrarily selected from among a single-crystal silicon film, a polycrystalline silicon film, an amorphous silicon film, a metal film, a compound semiconductor film, a superconductive film and the like. Or an element structure such as a MOSFET may be formed.




As shown in

FIG. 3C

, at least one kind of noble gas, hydrogen and nitrogen is ion-implanted into the porous layers


52


and


53


so as to form implanted layers


56


and


57


. When observing the implanted layers by a transmission electron microscope, formation of numberless micro-cavities can be seen, and accordingly the porosity enlarges. The charge condition of the implanted ions is not particularly limited. The acceleration energy is set such that the projection range corresponds to a depth at which the ion implantation is desired. Depending on the implantation amount, the size and the density of the micro-cavities to be formed are changed, but they are approximately no less than 1×10


14


/cm


2


and more preferably 1×10


15


/cm


2


. When setting the projection range deeper, channeling ion implantation may be employed. After the implantation, heat treatment is performed as necessary. In the case of the heat treatment atmosphere being oxidizing atmosphere, the pore walls are oxidized so that attention should be given to preventing the silicon region from being all changed into silicon oxide due to over oxidation.




As shown in

FIG. 3D

, after abutting two support substrates


58


and


59


and the surfaces of the non-porous thin films


54


and


55


of the first substrate with each other at room temperature, they are bonded to each other through anode bonding, pressurization, heat treatment or a combination thereof. As a result, the three substrates are firmly coupled with each other. Alternatively, the bonding may be performed in five plies with insulating thin plates interposed therebetween.




When single-crystal silicon is deposited, it is preferable to perform the bonding after oxidized silicon is formed on the surface of single-crystal silicon through thermal oxidation or the like. On the other hand, the support substrate can be selected from among a silicon substrate, a silicon substrate with a silicon oxide film formed thereon, a light transmittable substrate such as quartz, a sapphire substrate and the like, but not limited thereto as long as the surface serving for the bonding is completely flat. The bonding may be performed in three plies with an insulating thin plate interposed therebetween.




Subsequently, the substrates are divided at the ion-implanted layers


56


and


57


in the porous silicon layers


52


and


53


(FIG.


3


E). The structure of each of the two support substrate sides includes the porous silicon layer


52


,


53


, the non-porous thin film (for example, the single-crystal silicon layer)


54


,


55


and the support substrate


58


,


59


.




Further, the porous silicon layer


52


,


53


is selectively removed. In case of the non-porous thin film being single-crystal silicon, only the porous silicon layer


52


,


53


is subjected to the electroless wet chemical etching using at least one of the normal silicon etching liquid, hydrofluoric acid being the porous silicon selective etching liquid, a mixed liquid obtained by adding at least one of alcohol and aqueous hydrogen peroxide to hydrofluoric acid, buffered hydrofluoric acid, and a mixed liquid obtained by adding at least one of alcohol and aqueous hydrogen peroxide to buffered hydrofluoric acid, so that the film formed in advance on the porous layer of the first substrate remains on the support substrate. As described above in detail, only the porous silicon layer can be selectively etched using the normal silicon etching liquid due to the extensive surface area of porous silicon. Alternatively, the porous silicon layer


52


,


53


may be removed through selective polishing using the single-crystal silicon layer


54


,


55


as a polishing stopper.




In the case where the compound semiconductor layer is formed on the porous layer, only the porous silicon layer


52


,


53


is subjected to chemical etching using the etching liquid which has the greater etching speed for silicon relative to the compound semiconductor, so that the thickness-reduced single-crystal compound semiconductor layer


54


,


55


remains on the insulating substrate. Alternatively, the porous silicon layer


52


,


53


is removed through selective polishing using the single-crystal compound semiconductor layer


54


,


55


as a polishing stopper.




In

FIG. 3F

, the semiconductor substrates of the present invention are shown. On the support substrates, the non-porous thin films, such as the single-crystal silicon thin films


54


and


55


, are formed in large area all over the wafer, flatly and uniformly reduced in thickness, so that the two semiconductor substrates are simultaneously formed. The semiconductor substrates thus obtained can be suitably used also in view of production of the insulated electronic elements.




The first silicon single-crystal substrate


51


can be reused as a first silicon single-crystal substrate


51


after removing remaining porous silicon and after performing surface-flattening if the surface flatness makes it unusable. Alternatively, a non-porous thin film may be again formed without removing porous silicon so as to provide the substrate as shown in

FIG. 3B

, which is then subjected to the processes shown in

FIGS. 3C

to


3


F. The support substrates


58


and


59


are not necessarily identical with each other.




In a specific embodiment, any of the above surfaces can be treated to for smoothing purposes. Here, the final silicon surface may often be rough and needs finishing. The present surface treatment process removes surface roughness from the surface of the porous layer or silicon material. The film of silicon material is often rough and needs finishing. The rough surface for silicon wafers is often about two to eight nanometers RMS or greater. This roughness often should be removed before further processing. In a specific embodiment, the detached surface has a concentration of hydrogen bearing particles therein and thereon from the previous implanting step.




To smooth or treat the surface, the substrate is subjected to thermal treatment in a hydrogen bearing environment. Additionally, the substrate is also subjected to an etchant including a halogen bearing compound such as HCl, HBr, HI, HF, and others. The etchant can also be a fluorine bearing compound such as SF


6


or C


x


F


x


. In preferred embodiments, the present substrate undergoes treatment using a combination of etchant and thermal treatment in a hydrogen bearing environment. In a specific embodiment, the etchant is HCl gas or the like. The thermal treatment uses a hydrogen etchant gas. In some embodiments, the etchant gas is a halogenated gas, e.g., HCl, HF, HI, HBr, SF


6


, CF


4


, NF


3


, and CCl


2


F


2


. The etchant gas can also be mixed with another halogen gas, e.g., chlorine, fluorine. The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




In one embodiment, it is believed that the hydrogen particles in the detached surface improves the surface smoothing process. Here, the hydrogen particles have been maintained at a temperature where they have not diffused out of the substrate. In a specific embodiment, the concentration of hydrogen particles ranges from about 10


21


to about 5×10


22


atoms/cm


3


. Alternatively, the concentration of hydrogen particles is at least about 6×10


21


atoms/cm


3


. Depending upon the embodiment, the particular concentration of the hydrogen particles can be adjusted.




Still further in other embodiments, the present substrate undergoes a process of hydrogen treatment or implantation before thermal treatment purposes. Here, the substrate, including the detached film, is subjected to hydrogen bearing particles by way of implantation, diffusion, or any combination thereof. In some embodiments, where hydrogen has diffused out from the initial implant, a subsequent hydrogen treatment process can occur to increase a concentration of hydrogen in the detached film. The present hydrogen treatment process can occur for substrates made by way of other processes such as those noted below.




Moreover, the present technique for finishing the cleaved surface can use a combination of etchant, deposition, and thermal treatment to smooth the cleaved film. Here, the cleaved film is subjected to hydrogen bearing compounds such as HCl, HBr, HI, HF, and others. Additionally, the cleaved film is subjected to for example, deposition, during a time that the film is subjected to the hydrogen bearing compounds, which etch portions of the cleaved film. Using a silicon cleaved film for example, the deposition may occur by way of a silicon bearing compound such as silanes, e.g., Si


x


Cl


y


H


z


, SiH


4


, SiCl


x


, and other silicon compounds. Accordingly, the present method subjects the cleaved film to a combination of etching and deposition using a hydrogen bearing compound and a silicon bearing compound. Additionally, the cleaved surface undergoes thermal treatment while being subjected to the combination of etchant and deposition gases The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




An alternative embodiment will be described with reference to

FIGS. 4A

to


4


E. First, a single-crystal silicon substrate


100


is anodized to form a porous silicon layer


101


(FIG.


4


A). In this case, a thickness to be rendered porous is in the range from several micrometers to several tens of micrometers on one surface layer of the substrate. It may be arranged to anodize the whole silicon substrate


100


.




The method of forming porous silicon will be explained using

FIGS. 7A and 7B

. First, as the substrate, a p-type single-crystal silicon substrate


600


is prepared. An n-type may also be used. However, in this case, it is necessary that the substrate is limited to a low-resistance substrate or that the light is applied onto the surface of the substrate so as to facilitate generation of the holes. The substrate


600


is set in an apparatus as shown in FIG.


7


A. Specifically, one side of the substrate is in contact with a hydrofluoric acid solution


604


having therein a negative electrode


606


, while the other side of the substrate is in contact with a positive metal electrode


605


. On the other hand, as shown in

FIG. 7B

, a positive electrode


605


′ may also be provided in a solution


604


′. In any case, the substrate is first rendered porous from the negative electrode side abutting the hydrofluoric acid solution. As the hydrofluoric acid solution


604


, concentrated hydrofluoric acid (49% HF) is used in general. As diluted by pure water (H


2




0


), although depending on current values, etching occurs from a certain concentration so that it is not preferable. During anodization, bubbles are generated from the surface of the substrate


600


. Alcohol may be added as a surface active agent for effective removal of the bubbles. As alcohol, methanol, ethanol, propanol, isopropanol or the like is used. Instead of the surface active agent, an agitator may be used to agitate the solution to achieve anodization. The negative electrode


606


is made of a material, such as gold (Au) or platinum (Pt), which does not corrode relative to the hydrofluoric acid solution. A material of the positive electrode


605


may be metal which is used in general. On the other hand, since the hydrofluoric acid solution


604


reaches the positive electrode


605


when anodization is achieved relative to the whole substrate


600


, it is preferable to coat the surface of the positive electrode


605


with a metal film which is resistive to the hydrofluoric acid solution. The maximum current value for anodization is several hundreds of mA/cm


2


, while the minimum current value therefor is arbitrary, other than zero. This current value is determined in range where the good-quality epitaxial growth is achieved on the surface of porous silicon. In general, as the current value increases, the anodization speed increases and the density of the porous silicon layer decreases. That is, the volume of the pores increases. This changes the condition of the epitaxial growth.




On the porous layer


101


thus formed, a non-porous single-crystal silicon layer


102


is epitaxially-grown (FIG.


4


B). Subsequently, the surface of the epitaxial layer


102


is oxidized (including thermal oxidation) so as to form an SiO


2


layer


103


(FIG.


4


C). This is necessary because, if the epitaxial layer is directly bonded to the support substrate in the next process, impurities tend to segregate at the bonded interface and dangling bonds of atoms at the interface increase, which will cause the thin film device to be unusable. However, this process is not essential, but may be omitted in a device structure wherein such phenomena are not serious. The SiO


2


layer


103


works as an insulating layer of the SOI substrate and should be formed on at least one side of the substrate to be bonded. There are various ways to form of the insulating layer.




Upon oxidation, a thickness of the oxidized film is set to a value which is free of contamination taken into the bonded interface from the atmosphere.




Thereafter, the foregoing ion implantation is performed to form a layer with large porosity in the porous silicon layer


101


. The substrate


100


having the foregoing epitaxial surface with the oxidized surface and a support substrate


110


having an SiO


2


layer


104


on the surface are prepared. The support substrate


110


may be a silicon substrate whose surface is oxidized (including thermal oxidation), quartz glass, crystallized glass, an arbitrary substrate with SiO


2


deposited thereon, or the like. A silicon substrate without the SiO


2


layer


104


may also be used as the support substrate.




The foregoing two substrates are bonded together after cleaning them (FIG.


4


D). The cleaning is performed pursuant to the process of cleaning (for example, before oxidation) the normal semiconductor substrate. By pressurizing the whole substrate after the bonding, the bonding strength can be enhanced.




Subsequently, the bonded substrates are subjected to heat treatment. Although the higher temperature is preferable for the heat treatment, if it is too high, the porous layer


101


tends to cause structural change or the impurities contained in the substrate tend to be diffused into the epitaxial layer. Thus, it is necessary to select temperature and time which does not cause these problems. Specifically, about 600 to 1,100° C. is preferable. On the other hand, there is such are substrates that can not be subjected to thermal treatment at the high temperature. For example, in case of the support substrate


110


being made of quartz glass, it can be subjected to the thermal treatment only at the temperature no greater than 200° C. due to differences in the thermal expansion coefficients between silicon and quartz. If this temperature is exceeded, the bonded substrates may be separated or ruptured due to stress. The thermal treatment is sufficient as long as it can endure the stress upon grinding or etching of the bulk silicon 100 performed in the next process. Accordingly, even at the temperature no greater than 200° C., the process can be performed by optimizing the surface processing condition for activation.




Then, by the foregoing method, the substrates are separated into two at the porous silicon layer having the large porosity. The layer having the large porosity can be formed by altering current in the anodization, besides the ion implantation. Subsequently, the silicon substrate portion


100


and the porous portion


101


are selectively removed with the epitaxial layer


102


remaining (FIG.


4


E). In this fashion, the SOI substrate is obtained.




The following processes may be added to the foregoing processes:




(1) The thickness of the wall between the adjacent holes in the oxidized (preoxidation) porous silicon layer, of i.e. the pore internal walls of the porous layer, is very small, that is, several nanometers to several tens of nanometers. Thus, if the high-temperature process is applied to the porous layer upon formation of the epitaxial silicon layer or upon heat treatment after bonding, the pore wall may agglomerate an enlarge so that the pore wall may clog the pore and lower the etching speed. In view of this, after formation of the porous layer, a thin oxidized film is formed on the pore wall so as to suppress the enlargement of the pore wall. On the other hand, since it is necessary to epitaxially-grow the non-porous single-crystal silicon layer on the porous layer, it is necessary to oxidize only the surface of the pore inner wall such that the monocrystalline property remains inside the pore wall of the porous layer. It is preferable that the oxidized film is in the range of several angstroms to several tens of angstroms. The oxidized film of such a thickness is formed through heat treatment in an oxygen atmosphere at the temperature of 200° C. to 700° C., and more preferably 250° C. to 500° C.




(2) Thermal Treatment and Etching




In a specific embodiment, the present invention includes a method of applying a thermal treatment and etching to the surface or surfaces of the substrate for smoothing purposes. Here, small roughness on the silicon surface can be removed to obtain very smooth silicon surface. The combination of at least thermal treatment and etching can be performed, for example, after formation of the porous silicon layer and before formation of the epitaxial silicon layer. Apart from this, the thermal treatment and etching can be performed to the SOI substrate obtained after etching removal of the porous silicon layer. Through the thermal treatment and etching process performed before formation of the epitaxial silicon layer, a phenomenon that the pore surface is closed due to migration of silicon atoms forming the porous silicon surface. When the epitaxial silicon layer is formed in the state where the pore surface is closed, the epitaxial silicon layer with fewer crystal defects can be achieved. On the other hand, through the thermal treatment and etching process performed after etching of the porous silicon layer, the epitaxial silicon surface which was more or less roughened by etching can be smoothed out, and boron from the clean room inevitably taken into the bonded interface upon bonding and boron thermally diffused in the epitaxial silicon layer from the porous silicon layer can be removed.




As previously noted, to smooth or treat the surface, the substrate is subjected to thermal treatment in a hydrogen bearing environment. Additionally, the substrate is also subjected to an etchant including a halogen bearing compound such as HCl, HBr, HI, HF, and others. The etchant can also be a fluorine bearing compound such as SF


6


, C


x


F


x


. In preferred embodiments, the present substrate undergoes treatment using a combination of etchant and thermal treatment in a hydrogen bearing environment. In a specific embodiment, the etchant is HCl gas or the like. The thermal treatment uses a hydrogen etchant gas. In some embodiments, the etchant gas is a halogenated gas, e.g., HCl, HF, HI, HBr, SF


6


, CF


4


, NF


3


, and CCl


2


F


2


. The etchant gas can also be mixed with another halogen gas, e.g., chlorine, fluorine. The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be from an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




In one embodiment, it is believed that the hydrogen particles in the detached surface improves the surface smoothing process. Here, the hydrogen particles have been maintained at a temperature where they have not diffused out of the substrate. In a specific embodiment, the concentration of hydrogen particles ranges from about 10


21


to about 5×10


22


atoms/cm


3


. Alternatively, the concentration of hydrogen particles is at least about 6×10


21


atoms/cm


3


. Depending upon the embodiment, the particular concentration of the hydrogen particles can be adjusted.




Still further in other embodiments, the present substrate undergoes a process of hydrogen treatment or implantation before thermal treatment purposes. Here, the substrate, including the detached film, is subjected to hydrogen bearing particles by way of implantation, diffusion, or any combination thereof. In some embodiments, where hydrogen has diffused out from the initial implant, a subsequent hydrogen treatment process can occur to increase a concentration of hydrogen in the detached film. The present hydrogen treatment process can occur for substrates made by way of other processes such as those noted below.




Moreover, the present technique for finishing the cleaved surface can use a combination of etchant, deposition, and thermal treatment to smooth the cleaved film. Here, the cleaved film is subjected to hydrogen bearing compounds such as HCl, HBr, HI, HF, and others. Additionally, the cleaved film is subjected to for example, deposition, during a time that the film is subjected to the hydrogen bearing compounds, which etch portions of the cleaved film. Using a silicon cleaved film for example, the deposition may occur by way of a silicon bearing compound such as silanes, e.g., Si


x


Cl


y


H


z


, SiH


4


, SiCl


x


, and other silicon compounds. Accordingly, the present method subjects the cleaved film to a combination of etching and deposition using a hydrogen bearing compound and a silicon bearing compound. Additionally, the cleaved surface undergoes thermal treatment while being subjected to the combination of etchant and deposition gases The thermal treatment can be from a furnace, but is preferably from a rapid thermal processing tool such as an RTP tool. Alternatively, the tool can be from an epitaxial chamber, which has lamps for rapidly heating a substrate. In an embodiment using a silicon wafer and hydrogen gas, the tool can heat the substrate at a rate of about 10 Degrees Celsius/second and greater or 20 Degrees Celsius/second and greater, depending upon the embodiment.




An alternative embodiment will be described with reference to

FIGS. 5A

to


5


G. Numerals in

FIGS. 5A

to


5


G which are the same as those in

FIGS. 4A

to


4


E represent the same portions in

FIGS. 4A

to


4


E. In the embodiment shown in

FIGS. 4A

to


4


E, the surfaces of the two substrates to be bonded are the SiO


2


layer


103


and the SiO


2


layer


104


. However, both of these surfaces are not necessarily the SiO


2


layers, but at least one of them may be made of Si


0




2


. In this preferred embodiment, the surface of an epitaxial silicon layer


1102


formed on a porous silicon layer is bonded to the surface of an oxidized film


1104


formed on a silicon substrate


1110


, and the surface of an oxidized film


1103


formed by thermal oxidation of the surface of the epitaxial silicon layer


1102


is bonded to the surface of the silicon substrate


1110


which is not oxidized. In this preferred embodiment, the other processes can be performed as in the embodiment shown in

FIGS. 4A

to


4


E.




An alternative embodiment will be described with reference to

FIGS. 6A

to


6


G. Numerals in

FIGS. 6A

to


6


G which are the same as those in

FIGS. 4A

to


4


E represent the same portions in

FIGS. 4A

to


4


E. In this preferred embodiment, a substrate bonded to a substrate formed with an epitaxial silicon film is made of a glass material


1210


, such as quartz glass or blue glass. In this preferred embodiment, an epitaxial silicon layer


1102


is bonded to the glass substrate


1210


, and an oxidized film


1103


formed by thermal oxidation of the surface of the epitaxial silicon layer


1102


is bonded to the glass substrate


1210


. In this preferred embodiment, the other processes can be performed as in the embodiment shown in

FIGS. 4A

to


4


E.




Depending upon the embodiment, the present combination of thermal treatment and etching can be used to remove surface roughness of any of the detached films. The present invention can also use a combination of deposition, etching, and thermal treatment for other films in a porous film process. Further details of producing porous silicon materials are described in U.S. Pat. No. 5,854,123, assigned to Canon Kabushiki Kaisha.




In a specific embodiment, the silicon-on-insulator substrate undergoes a series of process steps for formation of integrated circuits thereon. These processing steps are described in S. Wolf, Silicon Processing for the VLSI Era (Volume 2), Lattice Press (1990), which is hereby incorporated by reference for all purposes.




Although the above description is in terms of a silicon wafer, other substrates may also be used. For example, the substrate can be almost any monocrystalline, polycrystalline, or even amorphous type substrate. Additionally, the substrate can be made of III/V materials such as gallium arsenide, gallium nitride (GaN), and others. The multi-layered substrate can also be used according to the present invention. The multi-layered substrate includes a silicon-on-insulator substrate, a variety of sandwiched layers on a semiconductor substrate, and numerous other types of substrates. Additionally, the embodiments above were generally in terms of providing a pulse of energy to initiate a controlled cleaving action. The pulse can be replaced by energy that is scanned across a selected region of the substrate to initiate the controlled cleaving action. Energy can also be scanned across selected regions of the substrate to sustain or maintain the controlled cleaving action. One of ordinary skill in the art would easily recognize a variety of alternatives, modifications, and variations, which can be used according to the present invention.




While the above is a full description of the specific embodiments, various modifications, alternative constructions and equivalents may be used. Therefore, the above description and illustrations should not be taken as limiting the scope of the present invention which is defined by the appended claims.




Although the above has been generally described in terms of a PIII system, the present invention can also be applied to a variety of other plasma systems. For example, the present invention can be applied to a plasma source ion implantation system. Alternatively, the present invention can be applied to almost any plasma system where ion bombardment of an exposed region of a pedestal occurs. Accordingly, the above description is merely an example and should not limit the scope of the claims herein. One of ordinary skill in the art would recognize other variations, alternatives, and modifications.




While the above is a full description of the specific embodiments, various modifications, alternative constructions and equivalents may be used. Therefore, the above description and illustrations should not be taken as limiting the scope of the present invention which is defined by the appended claims.



Claims
  • 1. A semiconductor substrate producing method comprising:forming a first porous silicon layer on at least one surface of a silicon substrate; forming a non-porous layer over said first porous layer; forming a second porous layer having a larger porosity than the first porous silicon layer at a constant depth from a surface of said first porous silicon layer, said second porous layer forming step comprising implanting ions into said first porous silicon layer with a given projection range; bonding said non-porous layer and a support substrate together, the support substrate being different than the silicon substrate; separating said silicon substrate into two portions at said second porous layer; removing at least said first porous layer provided over said support substrate to expose said non-porous layer; and smoothing said exposed non-porous layer by subjecting a surface of said non-porous layer using an etchant species and thermal treatment.
  • 2. The semiconductor substrate producing method according to claim 1 wherein said non-porous layer is formed on a surface of said first porous layer before said ion implanting step.
  • 3. The semiconductor substrate producing method according to claim 1 wherein said ions comprise of hydrogen or nitrogen or both.
  • 4. The semiconductor substrate producing method according to claim 2 wherein said separating step is performed by heat-treating said silicon substrate.
  • 5. The semiconductor substrate producing method according to claim 1 wherein said separating step is performed by pressurizing said silicon substrate in a direction perpendicular to a surface thereof.
  • 6. The semiconductor substrate producing method according to claim 1 wherein said separating step is performed by drawing said silicon substrate in a direction perpendicular to a surface thereof.
  • 7. The semiconductor substrate producing method according to claim 1 wherein said separating step is performed by applying a shearing force to said silicon substrate.
  • 8. The semiconductor substrate producing method according to claim 1 wherein said non-porous layer is made of single-crystal Si.
  • 9. The semiconductor substrate producing method according to claim 1 wherein said non-porous layer is made of single-crystal silicon having an oxidized silicon layer on a surface to be bonded.
  • 10. A semiconductor substrate producing method comprising:forming on a surface of a silicon substrate a first porous silicon layer, a second porous silicon layer and a third porous silicon layer, wherein the second porous silicon layer is located under the first porous silicon layer and has a porosity higher than the first porous silicon layer, and the third porous silicon layer is located under the second porous silicon layer and has a porosity lower than the second porous silicon layer; forming a non-porous monocrystalline semiconductor layer on the first porous silicon layer; bonding the non-porous monocrystalline semiconductor layer located on the silicon substrate to another substrate; and separating the silicon substrate and the other substrate at the second porous silicon layer so that the non-porous monocrystalline semiconductor layer remains on the other substrate; and removing the first porous silicon layer from the non-porous monocrystalline semiconductor layer; and subjecting a surface of the non-porous monocrystalline semiconductor layer with thermal energy and an etchant to remove a surface roughness from a first value to a second predetermined value.
  • 11. The semiconductor substrate producing method according to claim 10 wherein said forming step for forming said first, second and third porous silicon layers comprises a step for turning a surface portion of said silicon substrate porous.
  • 12. The semiconductor substrate producing method according to claim 11 wherein said second porous silicon layer is formed by means of ion implantation.
  • 13. The semiconductor substrate producing method according to claim 12 wherein said non-porous monocrystalline semiconductor layer is formed by epitaxial growth.
  • 14. A semiconductor substrate producing method comprising:forming on a surface of a silicon substrate a first porous silicon layer; implanting ions into the first porous silicon layer to form a second porous silicon layer having a porosity higher than the first porous silicon layer at a constant depth from a surface of the first porous silicon layer; forming a non-porous monocrystalline semiconductor layer on the first porous silicon layer; bonding the non-porous monocrystalline semiconductor layer located on the silicon substrate to another substrate; and separating the silicon substrate and the other substrate at the second porous silicon layer so that the non-porous monocrystalline semiconductor layer remains on the other substrate; and applying a combination of thermal treatment and an etchant to a surface of the non-porous monocrystalline semiconductor layer to reduce a surface roughness to a predetermined value.
  • 15. The method of claim 14 wherein the thermal treatment increases a temperature of the non-porous layer to about at least 1,000 Degrees Celsius.
  • 16. The method of claim 15 wherein the temperature is increased at least about 10 Degrees Celsius per second.
  • 17. The method of claim 15 wherein the temperature is increased at least about 20 Degrees Celsius per second.
  • 18. The method of claim 14 wherein the predetermined value is less than about two nanometers root mean square.
  • 19. The method of claim 14 wherein the etchant comprises a hydrogen bearing compound.
  • 20. The method of claim 14 wherein the etchant comprises a halogen bearing compound selected from at least Cl2, HCl, HBr, HI, and HF.
  • 21. The method of claim 14 wherein the etchant comprises a fluorine bearing compound.
  • 22. The method of claim 21 wherein the fluorine bearing compound is selected from SF6, CF4, NF3, and CCl2F2.
  • 23. A semiconductor substrate producing method comprising:forming a first porous silicon layer on at least one surface of a silicon substrate; forming a non-porous layer on said first porous layer; forming a second porous layer having a larger porosity than the first porous silicon layer within said first porous silicon layer by implanting ions into said first porous silicon layer; bonding said non-porous layer and a support substrate together, the support substrate being different than the silicon substrate; separating said silicon substrate into two portions at said second porous layer; removing said first and second porous layers provided over said support substrate to expose said non-porous layer; and smoothing said exposed non-porous layer by heating a surface of said non-porous layer within an atmosphere containing hydrogen and an etchant.
  • 24. A method of producing a semiconductor substrate, comprising:providing a silicon substrate having a porous silicon layer on a surface of said silicon substrate; providing a bonding substrate; bonding said silicon substrate and said bonding substrate together; separating said silicon substrate into two portions at said porous silicon layer, said bonding substrate separated from said silicon substrate having a first porous material on a surface of said bonding substrate, said silicon substrate separated from said bonding substrate having a second porous material on said surface of said silicon substrate; removing said porous material from at least one of said substrates to expose a non-porous layer of said at least one of said substrates; smoothing said exposed non-porous layer by heating a surface of said non-porous layer within an atmosphere containing hydrogen atoms and an etchant.
  • 25. The method of claim 24, wherein said at least one of said substrates is said bonding substrate and said removed porous material is said first porous material.
  • 26. The method of claim 24, wherein said porous silicon layer of said silicon substrate includes first and second porous layers.
  • 27. The method of claim 26, wherein said second porous layer is more porous than said first porous layer, said silicon substrate being separated into two portions at said second porous layer.
  • 28. The method of claim 27, wherein said second porous layer is provided within said first porous layer.
  • 29. The method of claim 24, wherein said at least one of said substrates is said silicon substrate and said removed porous material is said second porous material.
Parent Case Info

This application claims priority from provisional application Ser. No. 60/130,342, filed Apr. 21, 1999.

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Provisional Applications (1)
Number Date Country
60/130342 Apr 1999 US